[0001] The present invention relates to an image recording ink composition and a method
of using same.
[0002] In the field of ink jet recording, water-based inks have been mostly used from the
viewpoint of odor and safety. Currently employed water-based inks are solution type
inks prepared by dissolving various water-soluble dyes in water or a mixed solvent
of water and a water-soluble organic solvent and, if desired, by adding various additives
to the solution. An ink jet recording system using these inks has many excellent features
including: (1) the recording process is easy in nature of direct recording; (2) the
recording process is silent; (3) color recording is easily achieved; (4) high-speed
recording is feasible; (5) special paper is not required such that the operating cost
is low; and (6) ink is jetted in the form of fine droplets such that an image can
be formed with a high resolving power. Because of these advantages, ink jet recording
technology is being considered for future recording systems.
[0003] However, conventional ink jet recording techniques are disadvantageous in that (1)
the ink easily runs on paper (blurring) to deteriorate image quality; (2) the rate
of ink drying is low which results in smearing or tailing of the ink on non-image
areas (ink stain); (3) the fixing property of the ink is poor; (4) the nozzles and
ink passageways tend to become obstructed; (5) the image density is low; and (6) the
water resistance is poor.
[0004] In order to aleviate these disadvantages, it has been proposed to add a specific
surface active agent to an ink composition to thereby reduce the surface tension of
the ink and to increase absorption of the ink into the paper as disclosed in JP-A-55-29546
(the term "JP-A" as used herein means an "unexamined published Japanese patent application").
Furthermore, U.S. Patent 4,352,691 proposes the use of a strongly basic substance
to obtain an ink composition having a high pH value which, when transferred onto paper,
chemically dissolves a sizing agent added as a waterproofing agent or a pulp to thereby
control spread and absorption of ink dots in paper. JP-A-58-13675 teaches the addition
of polyvinylpyrrolidone having a molecular weight of 40,000 or more to an ink composition
to control spread of dots and absorption in paper. These proposals, however, did not
provide a complete solution to the above-described problems.
[0005] It is therefore an object of the present invention to provide an ink composition
for image formation which provides an image with sharp outlines free from blurring
and having a high density and a high gloss on a variety of printing materials including
fine paper, bond paper, PPC paper, OHP paper and recycled paper. This object is solved
by the image recording ink composition of independent claim 1 and the methods of independent
claims 24 and 26. Further advantageous features are evident from the dependent claims,
the following description, the drawing and the examples. The claims are to be understood
as a first non-limiting approach of defining the invention in general terms.
[0006] The present invention provides an ink composition for image formation which is rapidly
dried and fixed to thereby prevent staining and to achieve full color recording through
high-speed printing and overprinting of process colors.
[0007] The present invention further provides an ink composition for image formation having
excellent jetting stability and excellent preservability, and which does not cause
obstruction of nozzles and the ink passageway.
[0008] The present invention additionally provides an ink composition for image formation
which forms an image having excellent resistance to water and light.
[0009] The ink composition according to the invention is liquid and suitable for use in
an image recording printer.
[0010] The present invention provides an ink composition for image formation for use in
a printer for recording letters and images with a liquid ink, comprising water and
a coloring material and containing at least one water-insoluble component.
[0011] Fig. 1 schematically illustrates a dot of an ink composition of the present invention
formed on a printed material. In Fig. 1, printed material A comprises fibers 2 and
has formed thereon an ink dot having outline 1.
[0012] The ink composition of the present invention comprises water and a coloring material
and contains at least one water-insoluble component.
[0013] Coloring materials for use in the present invention include conventional water-soluble
dyes, oil-soluble dyes and dispersed dyes, as long as the coloring material does not
undergo change in hue or precipitate on addition of other ink components.
[0014] Specific examples of the water-soluble dyes include C.I. Direct Yellow 1, 8, 11,
12, 24, 26, 27, 28, 33, 39, 44, 50, 58, 85, 86, 87, 88, 89 and 98; C.I. Acid Yellow
1, 3, 7, 11, 17, 19, 23, 25, 29, 38, 44, 79, 127 and 144; C.I. Basic Yellow 1, 2,
11 and 34; C.I. Direct Red 1, 2, 4, 9, 11, 13, 17, 20, 23, 24, 28, 31, 33, 37, 39,
44, 46, 62, 63, 75, 79, 80, 81, 83, 84, 89, 95, 99, 113, 197, 201, 218, 220, 224,
225, 226, 227, 228, 229, 230 and 231; C.I. Acid Red 1, 6, 8, 9, 13, 14, 18, 26, 27,
35, 37, 42, 52, 82, 85, 87, 89, 92, 97, 106, 111, 114, 115, 118, 134, 158, 186, 249,
254 and 289; C.I. Basic Red 1, 2, 9, 12, 14, 17, 18 and 37; C.I. Direct Blue 1, 2,
6, 15, 22, 25, 41, 71, 76, 78, 86, 87, 90, 98, 163, 165 and 202; C.I. Acid Blue 1,
7, 9, 22, 23, 25, 29, 40, 41, 43, 45, 78, 80, 82, 92, 127 and 249; C.I. Basic Blue
1, 3, 5, 7, 9, 22, 24, 25, 26, 28 and 29; C.I. Direct Black 2, 7, 19, 22, 24, 26,
31, 32, 38, 51, 52, 56, 63, 71, 74, 75, 77, 108 and 154; C.I. Acid Black 1, 2, 7,
24, 26, 29, 31, 44, 48, 50, 52 and 94; and C.I. Basic Black 2 and 8.
[0015] Specific examples of oil-soluble dyes include C.I. Solvent Yellow 1, 2, 3, 4, 5,
6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 17, 19, 21, 26, 27, 29, 30, 35, 39, 40, 46, 49,
50, 51, 56, 61, 80, 86, 87, 89 and 96; C.I. Solvent Red 1, 2, 3, 8, 16, 17, 18, 19,
20, 22, 23, 24, 25, 26, 27, 30, 49, 52, 59, 60, 63, 67, 68, 81, 82, 84, 100 and 121;
C.I. Solvent Blue 2, 6, 11, 12, 15, 20, 25, 30, 31, 32, 35, 36, 55, 58, 71, 72 and
73; and C.I. Solvent Black 3, 5, 7, 10, 11, 12, 13, 22 and 23.
[0016] Specific examples of dispersed dyes include C.I. Disperse Yellow 1, 3, 4, 7, 8 and
31; C.I. Disperse Red 1, 4, 5, 7, 11 and 12; C.I. Disperse Blue 1, 3, 5, 6, 7 and
27; and C.I. Disperse Black 1, 2, 10, 26, 27 and 28.
[0017] A pigment can also be used as the coloring material of the present invention, and
useful pigments include inorganic pigments (e.g., carbon black) and organic pigments
(e.g., insoluble azo pigments, soluble azo pigments, phthalocyanine pigments, isoindolinone
pigments, quinacridone pigments, perinone pigments and perylene pigments). Processed
pigments obtained by treating the surface of pigment particles with resins, etc. (e.g.,
graft carbon) may also be used.
[0018] Specific examples of inorganic pigments include acidic carbon blacks (MA-100, #1000,
MA-7, MA-8 and MA-11, manufactured by Mitsubishi Kasei Corporation; Raven 1255, 1250,
1060, 1035, 1040, 1020, 1000 and 760, manufactured by Columbian Carbon Japan Ltd.)
and graft carbon (GPT-505P manufactured by Ryoyu Kogyo).
[0019] In order to improve dispersion stability of ink composition during storage and recorded
image quality, the acidic carbon blacks are preferably used.
[0020] Specific examples of organic pigments include C.I. Pigment Yellow 1, 2, 3, 5, 12,
13, 14, 15, 17 and 83; C.I. Pigment Red 1, 2, 3, 4, 5, 7, 9, 12, 22, 23, 37, 38, 81
and 146; C.I. Pigment Blue 1, 2, 15, 16 and 17; and C.I. Pigment Black 1.
[0021] The colored particles or pigment particles are preferably pulverized to have a particle
diameter of not more than 1.0 µm.
[0022] The coloring material is preferably used in an amount of from 1 to 16% by weight,
more preferably from 1 to 10% by weight, particularly preferably from 1.5 to 6% by
weight, based on the ink composition. If the amount is less than 1% by weight, it
is difficult to obtain the desired hue and density. If the addition amount exceeds
16% by weight, the ink tends to cause obstruction or reduce the storage stability.
[0023] The dyes are preferably used in an amount of from 1 to 6% by weight based on the
ink composition.
[0024] The pigments are preferably used in an amount of from 1 to 10% by weight, more preferably
from 1.5 to 6% by weight, based on the ink composition.
[0025] When a dye is used as the coloring material, the dye is used together with the water-insoluble
component. For example, the dye can be impregnated, chemically adsorbed or loaded
into a water-insoluble polymer dispersion particle.
[0026] Where a pigment is used as a coloring material, the pigment itself can be used as
a water-insoluble component by dispersing the same in water. Alternatively, the pigment
can be used together with one or more other water-insoluble components.
[0027] The water-insoluble polymer other than a coloring material for use as a water-insoluble
component of the present invention includes homo- or copolymer resin emulsions of
vinyl esters, acrylic esters, methacrylic esters, styrenes, olefins, or monomers having
a hydrophilic functional group, e.g., an amino group, a carboxyl group, an amido group,
a hydroxyl group, etc.; organic ultrafine particles having an internal three-dimentional
cross-linked structure; microemulsions; colloidal dispersions; and natural or synthetic
wax emulsions, e.g., paraffin wax, microcrystalline wax, polyethylene wax, and carnauba
wax. The organic ultrafine particles having an internal three-dimentional cross-linked
structure are described, for example, in K. Ishii et. al.; Proc. ACS Div. PMSE, 52,
448 (1985), S. Ishikawa et. al.; Prog. in Org. Coatings, 15, 373 (1988), and K. Ishii
et. al.; XIX, FATIPEC KONGRESS, vol. IV, p.187 (1988). With respect to the conventional
resin emulsion, particles therein are fused with each other due to evaporation of
water to form a film. However, the organic ultrafine particles having an internal
three-dimentional cross-linked structure do not form a film due to a fusion, although
they may be agglomerated, and an emulsion thereof can be re-disparsed. Accordingly,
the emulsion of the organic ultrafine particles insures an effect of preventing obstruction
of nozzles and the ink passageway, without adding a large amount of humectant. Further,
because a viscosity of the emulsion of the organic ultrafine particles increases due
to evaporation of water, the emulsion improves the fixing properties of coloring material
on printing paper and prevents running (blur). Among the microemulsions, ultramicroemulsions
(PB-300 series manufactured by Kao Corporation) are preferred because they are stable
at low temperature (0°C) and high temperature (50°C) and improve storage stability
of ink composition. Among the colloidal dispersions, water sols (CD-520, CD-530 and
CD-540, manufactured by Dainippon Ink & Chemicals, Inc.) are preferred. These water-insoluble
components other than coloring material can be prepared by, for example, pulverizing
a polymer obtained by emulsion polymerization, suspension polymerization, dispersion
polymerization or other polymerization processes. Furthermore, inorganic ultrafine
particles such as a colloidal silica ("Adelite" manufactured by Asahi Denka Kogyo
K.K.), etc. can be used.
[0028] The above described resin emulsion can be used as a water-insoluble colored emulsion
by dying with a dye. Furthermore, the resin emulsion can be added as the water-insoluble
component other than a coloring material.
[0029] The water-insoluble resin emulsion is preferably used in an amount of from 1 to 20%
by weight calculated as a solid content, based on the ink composition.
[0030] The water-insoluble component is preferably used in an amount of from 2 to 30% by
weight based on the ink composition.
[0031] The water-insoluble component preferably has a particle diameter of from 0.001 µm
to 10 µm. If the particle diameter exceeds 10 µm, the water-insoluble component tends
to precipitate.
[0032] The ink composition of the present invention necessarily contains water. Other solvents
which may be used for preparing the ink composition of the present invention include
water and water-soluble organic solvents, such as alkyl alcohols having from 1 to
4 carbon atoms, ketones or keto alcohols, ethers, polyalkylene glycols, alkylene glycols
having from 2 to 6 carbon atoms in the alkylene moiety thereof, glycerin, lower alkyl
ethers of polyhydric alcohols, N-methyl-2-pyrrolidone, and triethanolamine. The water
for use in the present invention is ion-exchange treated water. Water-soluble organic
solvents used to prepare the ink composition of the present invention may be removed
by evaporation.
[0033] Water or the ion-exchanged water is preferably used in an amount of from 50 to 95%
by weight, more preferably from 60 to 90% by weight, based on the ink composition.
[0034] The calcium ion and magnesium ion concentrations in the ion-exchanged water are preferably
at most 5 ppm.
[0035] The ink composition of the present invention may contain a water-soluble resin in
combination with the water-insoluble component in order to improve fixing properties,
to adjust the viscosity and to improve drying properties. Examples of useful water-soluble
resins include glue, gelatin, casein, albumin, gum arabic, alginic acid, methyl cellulose,
carboxymethyl cellulose, polyethylene oxide, hydroxyethyl cellulose, polyvinyl alcohol,
polyacrylic acid, polyvinyl ether, and polyvinylpyrrolidone.
[0036] The water-soluble resin is preferably used in an amount of from 0.01 to 10% by weight,
more preferably from 0.1 to 5% by weight, based on the ink composition.
[0037] The ink composition of the present invention other than those wherein a water-soluble
dye is dissolved in water may further comprise a penetrant in order to permeate a
solvent of the ink composition alone into the printed material. Use of the penetrant
retains the coloring material on the surface of the printed material to thereby impart
faster drying properties. Examples of the penetrant for use in the present invention
include alkali metal hydroxides (e.g., lithium hydroxide, sodium hydroxide and potassium
hydroxide), various surface active agents, methyl alcohol, ethyl alcohol, n-propyl
alcohol, iso-propyl alcohol, n-butyl alcohol, diethylene glycol monobutyl ether, triethylene
glycol monomethyl ether, N-methyl-2-pyrrolidone, and 1,3-dimethyl-2-imidazolidinone.
[0038] The penetrant is preferably used in an amount of from 0.005 to 10% by weight, more
preferably from 0.01 to 5% by weight, based on the ink composition.
[0039] If desired, the ink composition of the present invention may further contain various
known additives for printing inks such as dispersing agents, viscosity modifiers,
surface-tension modifiers, specific-resistance modifiers, pH adjustors, antifungal
agents, chelating agents, etc.
[0040] The ink composition of the present invention preferably has a viscosity of not more
than 30 mPa·s in the vicinity of a jet nozzle at a working temperature of from 0°
to 50°C, taking the stability of the ink supply to a recording head and the stability
of jetting ink droplets in high-speed recording into consideration. To achieve a higher
speed of recording, a viscosity of from 1.5 to 20 mPa·s is particularly preferred.
The term "high-speed recording" means an ability of printing letters at a speed of
2 pages (letter size) per minute.
[0041] The ink composition of the present invention preferably has a surface tension of
40 dyne/cm or more. An ink composition having a surface tension of less than 40 dyne/cm
tends to blur on paper having a low degree of sizing, to thereby reduce the printing
resolution.
[0042] The contact angle of the ink composition of the present invention to a material to
be transferred is preferably at least 60°, more preferably at least 72°.
[0043] Means for uniformly dispersing the coloring component into a dispersing medium include
a method of utilizing the effect of an electric double layer at the interface of the
coloring material and the dispersion medium, a method of utilizing the protective
action of an adsorption layer formed by a surface active agent or a high molecular
weight polymeric protective colloid, a method of chemically bonding a high molecular
weight polymer having a reactive functional group soluble in the dispersing medium
and the surface of a coloring component, and a method of chemically bonding a suitable
coupling agent with the surface of a coloring component. Because water having a high
polarity is used as a dispersion medium of the present invention, stable dispersability
can be obtained.
[0044] In the preparation of the ink composition of the present invention, dispersion of
the pigment can be carried out by using a pulverizer or a micro-atomizer, such as
a ball mill, sand mill, attritor, roll mill, agitator mill, Henschel mixer, colloid
mill, ultrasonic homogenizer, high pressure homogenizer, pearl mill, jet mill, angmill,
a mechanofusion apparatus (manufactured by Hosokawa Micron), and a hybridization apparatus
(manufactured by Nara Kikai Seisakusho).
[0045] If desired, the dispersion of the pigment is passed through a filter, etc., which
filtering may be carried out under reduced pressure, or under pressure, to remove
large particles, dust, contaminants, etc., or the dispersion may be stirred or mixed
to obtain a final ink composition.
[0046] In drying and fixing of the image recording ink of the present invention, a heat
fixing means such as hot air, a heating roll, and infrared rays may be used, if desired.
[0047] The ink composition for image formation of the present invention can be used in a
conventional on-demand type (so-called Kyser type and thermal ink jet type) ink jet
system and in an ink mist system in which an ink mist is generated by ultrasonic wave,
etc. The ink composition of the present invention is also applicable to an ink jet
system comprising a nozzle plate having a plurality of nozzles and a piezoelectric
transducer which is fixed close to the nozzle plate, being soaked in the ink and constituting
an independently driven oscillator, wherein an electrical voltage is applied to the
piezoelectric transducer to impart a varied pressure to the ink inside the nozzle
plate while insulating the part of the transducer in contact with the ink. As a result,
the ink is jetted from the nozzles to achieve printing.
[0048] When a recording is carried out using the above-described recording system at a
flying speed of at least 10 m/sec and at an ink amount of at most 0.2 µg/dot, high-quality
recording can be made, and rapid ink drying properties of a drying speed of at most
10 sec can be realized. Further, a recording method wherein one dot is composed of
2 to 4 microdots of at most 0.05 µg/dot is more preferred.
[0049] The present invention is now illustrated in greater detail with reference to the
following Examples and Comparative Examples, but it should be understood that the
present invention is not deemed to be limited thereto. All the percents are by weight
unless otherwise indicated.
[0050] Physical properties of the ink compositions prepared in the Examples below were determined
as follows.
a) Viscosity:
[0051] The stationary viscosity at 20°C was measured with a Flude Spectrometer manufactured
by Rheometrix Far East Co.
b) Surface Tension:
[0052] The surface tension was measured with a tensiometer manufactured by Kyowa Kaimen
Kagaku.
c) Average Particle Size:
[0053] The average particle size was obtained from the particle size distribution as determined
by an ξ-potentiometer of a laser light scattering system "ELS 800" manufactured by
Ohtsuka Denshi K.K.
d) Contact Angle:
[0054] The contact angle was measured with an automatic contact angle meter (CZ-A type)
manufactured by Kyowa Kaimen Kagaku.
EXAMPLE 1 |
C.I. Solvent Black 23 |
3% |
Methyl methacrylate |
11% |
n-Butyl acrylate |
7% |
Glycidyl methacrylate |
2% |
Ion-exchanged water |
67.5% |
Sodium dodecylsulfate |
1% |
Potassium persulfate |
0.5% |
Glycerin |
8% |
[0055] In a flask equipped with a temperature controller, a stirrer, an inlet for nitrogen,
and a dropping funnel, the atmosphere of which had been displaced with nitrogen, were
added the sodium dodecylsulfate and ion-exchanged water. After heating the solution
to 70°C, a monomer mixture comprising the methyl methacrylate, n-butyl acrylate, and
glycidyl methacrylate was dropwise added thereto over 2 hours while dropwise adding
the potassium persulfate over 3 hours.
[0056] After completion of the addition of the potassium persulfate, the temperature was
elevated to 80°C. The mixture was stirred for 1 hour, followed by filtration through
a filter having a pore size of 1.2 µm under reduced pressure to prepare a resin emulsion
having an average particle size of 0.8 µm.
[0057] To the resulting resin emulsion was added a solution of the C.I. Solvent Black 23
dissolved in acetone, and the mixture was stirred for two hours. After the acetone
was removed by evaporation, the glycerin was added to the resulting mixture followed
by stirring for 30 minutes. The mixture was filtered through a filter having a pore
size of 1.2 µm under reduced pressure to obtain a recording ink composition having
a surface tension of 48 dyne/cm.
EXAMPLE 2
[0058] The same procedure as in Example 1 was repeated except for adding, as a penetrant,
5% of methyl alcohol to the recording ink composition of Example 1 to obtain a recording
ink composition having surface tension of 42 dyne/cm.
EXAMPLE 3 |
Carbon black (MA-100 manufactured by Mitsubishi Kasei Corporation) |
6% |
Acrylic resin (Aron A-20LL manufactured by Toagosei Chemical Industry Co., Ltd.) |
3% |
Glycerin |
10% |
Ion-exchanged water |
80% |
[0059] The acrylic resin and carbon black were kneaded in a roll mill, and the mixture and
the ion-exchanged water were dispersed in a sand mill for 10 hours. The mixture was
transferred to a stirring machine, and the glycerin was added thereto. The mixture
was filtered through a filter having a pore size of 1 µm under reduced pressure to
prepare a recording ink composition having an average particle size of 0.08 µm and
a surface tension of 58 dyne/cm.
EXAMPLE 4
[0060] The same procedure as in Example 3 was repeated except for adding, as a penetrant,
5% of N-methyl-2-pyrrolidone to the recording ink composition of Example 3 to obtain
a recording ink composition having surface tension of 49 dyne/cm.
EXAMPLE 5 |
Carbon black (MA-100 manufactured by Mitsubishi Kasei Corporation) |
6% |
Polyvinylpyrrolidone (K=15) |
3% |
Nonionic dispersing agent (Demol N manufactured by Kao Corporation) |
0.8% |
Glycerin |
10% |
Ion-exchanged water |
79.2% |
[0061] The ion-exchanged water, polyvinylpyrrolidone, carbon black, and dispersing agent
were dispersed in a paint shaker for 15 hours. The dispersion was transferred to a
stirring machine, and the glycerin was added thereto. The mixture was passed through
a filter having a pore size of 1 µm under reduced pressure to prepare a recording
ink composition having an average particle size of 0.2 µm and a surface tension of
63 dyne/cm.
EXAMPLE 6
[0062] The same procedure as in Example 5 was repeated except for adding, as a penetrant,
5% of 1,3-dimethyl-2-imidazolidinone to the recording ink composition of Example
5 to obtain a recording ink composition having surface tension of 51 dyne/cm.
EXAMPLE 7 |
Carbon black (MA-100 manufactured by Mitsubishi Kasei Corporation) |
6% |
Ultramicroemulsion (solid content: 20%, PB-300 manufactured by Kao Corporation) |
30% |
Glycerin |
15% |
Ion-exchanged water |
50% |
[0063] The ion-exchanged water, nonionic dispersing agent, and carbon black were dispersed
in a sand mill for 10 hours, and the ultramicroemulsion and the glycerin were added
thereto, followed by stirring for 1 hour. The mixture was passed through a filter
having a pore size of 1 µm under reduced pressure to prepare a recording ink composition
having an average particle size of 0.08 µm and a surface tension of 48 dyne/cm.
EXAMPLE 8
[0064] The same procedure as in Example 7 was repeated except for adding, as a penetrant,
5% of diethylene glycol monobutyl ether to the recording ink composition of Example
7 to obtain a recording ink composition having surface tension of 41 dyne/cm.
EXAMPLE 9 |
C.I. Direct Black 154 |
3% |
Organic ultrafine particles (solid content: 25%) (Microgel manufactured by Nippon
Paint K.K.) |
40% |
Ion-exchanged water |
52% |
Glycerin |
6% |
[0065] The C.I. Direct Black 154 was dissolved in the ion-exchanged water, and the organic
ultrafine particles (solid content: 25%) and glycerin were added to the solution,
followed by stirring in a stirring machine for 1 hour. The mixture was passed through
a membrane filter having a pore size of 0.8 µm to prepare a recording ink composition
having an average particle size of 0.03 µm and a surface tension of 45 dyne/cm.
EXAMPLE 10 |
C.I. Pigment Yellow 12 |
6% |
Polyvinylpyrrolidone |
4% |
Nonionic dispersing agent (Demol N manufactured by Kao Corporation) |
4% |
Glycerin |
10% |
Ion-exchanged water |
76% |
C.I. Pigment Red 146 |
6% |
Polyvinylpyrrolidone |
4% |
Nonionic dispersing agent (Demol N manufactured by Kao Corporation) |
4% |
Glycerin |
10% |
Ion-exchanged water |
76% |
C.I. Pigment Blue 15 |
6% |
Polyvinylpyrrolidone |
4% |
Nonionic dispersing agent (Demol N manufactured by Kao Corporation) |
4% |
Glycerin |
10% |
Ion-exchanged water |
76% |
[0066] Each of the yellow, magenta, and cyan pigments, polyvinylpyrrolidone, and nonionic
dispersing agent were dispersed in a paint shaker for 20 hours. Each dispersion was
transferred to a stirring machine, and glycerin was added thereto, followed by filtration
through a filter having a pore size of 1 µm under reduced pressure to prepare three
recording color ink compositions each having an average particle size of 0.2 µm and
a surface tension of 61 dyne/cm.
EXAMPLE 11
[0067] The same procedure as in Example 10 was repeated except for adding, as a penetrant,
1% of sodium dioctylsulfosuccinate to the recording color ink compositions of Example
10 to obtain three recording color ink compositions each having surface tension of
43 dyne/cm.
COMPARATIVE EXAMPLE 1 AND 2
[0068] For comparison, a commercially available ink for an on-demand ink jet printer (Comparative
Example 1) and a commercially available ink for a bubble jet printer (Comparative
Example 2) were used. The composition of each of the commercially available inks is
shown below.
Comparative Example 1 |
C.I. Direct Black 19 |
2% |
Glycerin |
15% |
Ion-exchanged water |
83% |
Surface Tension |
48 dyne/cm |
Comparative Example 2 |
C.I. Direct Black 19 |
2% |
Diethylene glycol |
10% |
Ethanol |
5% |
Ion-exchanged water |
83% |
Surface Tension |
46 dyne/cm |
[0069] Viscosity, surface tension, and average particle size of each of the ink compositions
of Examples 1 to 11 and Comparative Examples 1 and 2 are shown in Table 1 below.
[0070] In order to test printability of each of the recording ink compositions, letters
or graphics were printed with the ink composition on (A) fine paper for general use,
(B) bond paper, (C) PPC paper, (D) recycled paper, or (E) general OHP sheets by the
use of a commercially available on-demand ink jet printer (HG-2500 manufactured by
Seiko Epson Corporation) and a multihead produced for experimental use in the manner
as disclosed, for example, in U.S. Patent 4,072,959 (jet orifice diameter: 30 µm;
piezo-oscillator driving voltage: 40 V; driving frequency: 8 kHz). The resulting recorded
image was evaluated according to the following rating system.
1) Blur:
[0071] The extent of blurring of the recorded image was observed both visually (nakedcye)
and under microscopically (100X magnification and 400X magnification).
Excellent ... Dots were fixed on fibers without blurring along the fibers under microscopic
inspection..
Good ........ Slight blur was observed along the fibers under microscopic inspection,
but was visually imperceptible.
Medium ...... Slight blurring was observed visually.
Poor ........ Considerable blurring was visually observed, and the image had a jaggy
edge.
2) Rapid Drying Properties:
[0072] Ten seconds, 30 seconds and 60 seconds after recording, the recorded image was scratched
with an edge of paper.
Excellent ... No stain was observed after 10 seconds.
Good ........ No stain was observed after 30 seconds
Medium ...... No stain was observed after 60 seconds
Poor ........ Stain was observed after 90 seconds
3) Fixing Properties:
[0073] One hour after recording, the surface of the recorded image was repeatedly scratched
back and forth with a clip under a load of 200 g/cm until a stain appeared.
Excellent ... No staining observed after 30 or more reciprocal scratches.
Good ........ Staining first observed after 20 to 30 reciprocal scratches.
Poor ........ Staining first observed prior to 20 reciprocal scratches.
4) Obstruction:
[0074] The ink composition was filled in the above-described ink jet printer and left to
stand at 50°C for 1 month with no cap on the nozzle.
Good ........ Printing could be conducted right from the without further preparation.
Medium ...... Printing could be conducted after the ink was circulated for cleaning.
Poor ........ Printing could not be conducted.
5) Ink Preservability:
[0075] The ink composition was sealed in a sample bottle and stored at 50°C for 6 months.
Any change, such as the generation of foreign matter or offensive odor, or the formation
of agglomerates or precipitates, was observed.
Excellent ... No change.
Good ........ A precipitate was formed but was easily re-dispersed.
Poor ........ A precipitate was formed and could not be re-dispersed.
6) Recording Density:
[0076] The reflective optical density (OD) of the recorded image was measured with a Macbeth
densitometer (TR-927 type).
7) Water-Resistance:
[0077] A printed sheet 1 hour after printing was immersed in water for 5 minutes, and the
printed sheet thus treated was evaluated for running of the ink.
Good ... No running was observed.
Poor ... Running was observed.
8) Gloss:
[0078] The specular gloss at an angle of 75° was measured with a digital glossmeter (manufactured
by Murakami Shikisai Gijutsu Kenkyusho).
Good ..... 80 or more
Medium ... 51 to 79
Poor ..... 50 or less
9) printability on OHP Paper:
[0079] Good ... Printable
Poor ... Unprintable
10) Light Resistance:
[0080] The recorded image was irradiated with the light of a xenon lamp (400 W) for 100
hours, with the distance between a sample and the lamp being 25 cm, and fading was
determined using a blue scale in accordance with JIS L 0841.
Good ... At least fourth grade
Poor ... Less than fourth grade
[0082] As can be seen from the results of Table 2, the recording ink compositions of Examples
1 to 6 of the present invention are markedly superior to the conventional inks for
an ink jet recording system in terms of image quality (blur, density, gloss, water
resistance and light resistance), rapid drying properties, fixing properties, freedom
from obstruction, and ink preservability.
[0083] According to the above described Examples of the present invention, on printing,
the coloring component of the ink composition of the present invention is adhered
in place on the printing material by the cohesive force of the water-insoluble component,
such that the ink is solidified and fixed to form dots having sharp outlines as shown
in Fig. 1.
[0084] As described above, the ink composition of the present invention comprising water
and a coloring material and containing at least one water-insoluble component to thereby
obtain have a heterogeneous phase, exhibits satisfactory drying properties and fixing
properties and provides a clear and high density recorded image having excellent resistance
to water and light without causing running (blur). Also, the ink composition of the
present invention does not cause obstruction in a printing machine and has excellent
preservability.
[0085] Furthermore, the ink composition of the present invention is adaptable to high-speed
and high-quality printing on general OHP paper, which has not hitherto been employable
in a conventional ink jet recording system.
[0086] Also, the satisfactory drying and fixing properties of the ink composition of the
present invention provides for multicolor printing to obtain a full color image having
high resolution by using three process color inks.
[0087] In addition, the ink composition of the present invention can be used for printing
on recycled paper which is expected to became readily available in the market.
[0088] While the invention has been described in detail and with reference to specific embodiments
thereof, it will be apparent to one skilled in the art that various changes and modifications
can be made therein without departing from the spirit and scope thereof.
1. An image recording ink composition for use in a printer for recording letters and
images with a liquid ink, comprising water and a coloring material and containing
at least one water-insoluble component.
2. An image recording ink composition as in claim 1, wherein said ink composition
comprises water, a dye and a water insoluble resin emulsion.
3. An image recording ink composition as in claim 1, wherein said ink composition
comprises water and a pigment.
4. An image recording ink composition as in claim 3, further comprising a penetrant.
5. An image recording ink composition as in one of claims 3 or 4, further comprising
a water-insoluble resin emulsion.
6. An image recording ink composition as in one of claims 3 or 4, further comprising
a water-soluble resin.
7. An image recording ink composition as in claim 1, wherein said ink composition
comprises water and a colored water-insoluble resin emulsion.
8. An image recording ink composition as in one of the preceding claims, wherein said
ink composition has a viscosity of not more than 30 mPa·s, preferably of from 1.5
to 20 mPa·s, at a temperature of from 0° to 50°C.
9. An image recording ink composition as in one of the preceding claims, wherein said
ink composition has a surface tension of 40 dyne/cm or more.
10. An image recording ink composition as in one of the preceding claims, wherein
said ink composition constitutes a heterogeneous phase.
11. An image recording ink composition as in one of the preceding claims, wherein
said coloring material has a particle diameter of not more than 1.0 µm.
12. An image recording ink composition as in one of claims 1 to 5 and 7 to 11, wherein
said at least one water-insoluble component is a water-insoluble polymer dispersion
particle.
13. An image recording ink composition as in claim 12, wherein said water-insoluble
polymer dispersion particle is selected from homo- or copolymer resin emulsions of
vinyl esters, acrylic esters, methacrylic esters, styrenes, olefins, or monomers having
a hydrophilic functional group; organic ultrafine particles having an internal three-dimensional
cross-linked structure; microemulsions; colloidal dispersions; and natural or synthetic
wax emulsions.
14. An image recording ink composition as in claim 3 or one of the claims dependent
on claim 3, wherein said pigment is selected from carbon black, insoluble azo pigments,
soluble azo pigments, phthalocyanine pigments, isoindolinone pigments, quinacriodone
pigments, perinone pigments and perylene pigments.
15. An image recording ink composition as in claim 14, wherein the carbon black is
an acidic carbon black.
16. An image recording ink composition as in one of the preceding claims, wherein
the ink composition contains water in the amount of 50 to 95% by weight, preferably
in the amount of 60 to 90% by weight.
17. An image recording ink composition as in one of the preceding claims, wherein
the ink composition contains the coloring material in the amount of 1 to 16% by weight,
preferably in the amount of 1 to 10% by weight, and most preferably in the amount
of 1.5 to 6% by weight.
18. An image recording ink composition as in one of the preceding claims, wherein
the ink composition contains the water-insoluble component in the amount of 2 to 30%
by weight.
19. An image recording ink composition as in claim 2 or one of the claims dependent
on claim 2, wherein the ink composition contains the dye in the amount of 1 to 6%
by weight.
20. An image recording ink composition as in claim 3, wherein the ink composition
contains the pigment in the amount of 1 to 10% by weight, preferably in the amount
of 1.5 to 6% by weight.
21. An image recording ink composition as in claim 4 or one of the claims dependent
on claim 4, wherein the ink composition contains the penetrant in the amount of 0.005
to 10% by weight, preferably in the amount of 0.01 to 5% by weight.
22. An image recording ink composition as in claim 2 or 5 or one of the claims dependent
on claims 2 or 5, wherein the ink composition contains the water-insoluble resin emulsion
in the amount of 1 to 20% by weight calculated as a solid content and/or wherein the
water-insoluble resin emulsion is selected from organic ultrafine particles having
an internal three-dimensional cross-linked structure and ultramicroemulsions.
23. An image recording ink composition as in claim 6 or one of the claims dependent
on claim 6, wherein the ink composition contains the water-soluble resin in the amount
of 0.01 to 10% by weight, preferably in the amount of 0.1 to 5% by weight.
24. A method for recording letters and images using an ink composition comprising
water and a coloring material and containing at lest one water-insoluble component,
according to one of the preceding claims, comprising jetting droplets of the ink composition
onto a printing material.
25. A method for recording letters and images as in claim 24, wherein the contact
angle of the ink composition to the printing material is at least 60°, preferably
at least 72°.
26. An ink jet recording method, especially according to claim 24 or 25, comprising
jetting an ink composition comprising water and a coloring material and containing
at least one water-insoluble component according to one of claims 1 to 23 from nozzles
at a flying speed of at least 10 m/sec and at an ink amount of at most 0.2 µg/dot.